Canonical Allele Identifier: CA2210074733

Gene: ABCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16044465T= , CM000678.2:g.16044465T=	GRCh38
NC_000016.9:g.16138322T= , CM000678.1:g.16138322T=	GRCh37
NC_000016.8:g.16045823T=	NCBI36
NG_028268.1:g.99889T=
NG_028268.2:g.99889T=

Transcript Alleles

HGVS	Amino-acid Change
NM_004996.4:c.825T= MANE Select	NP_004987.2:p.Val275=
ENST00000399410.8:c.825T= MANE Select	ENSP00000382342.3:p.Val275=
NM_004996.3:c.825T=	NP_004987.2:p.Val275=
ENST00000399408.6:c.-154T=	ENSP00000382340.3:n.-154T=
ENST00000399408.7:c.825T=	ENSP00000382340.4:p.Val275=
ENST00000399410.7:c.825T=	ENSP00000382342.3:p.Val275=
ENST00000572882.2:c.520T=
ENST00000572882.3:c.825T=	ENSP00000461615.2:p.Val275=
ENST00000574224.1:n.425T=
ENST00000574224.2:n.900T=
ENST00000677164.1:c.699T=	ENSP00000502873.1:p.Val233=
ENST00000678422.1:c.825T=	ENSP00000503954.1:p.Val275=
ENST00000679043.1:n.777T=
XM_011522497.1:c.801T=	XP_011520799.1:p.Val267=
XM_011522498.1:c.879T=	XP_011520800.1:p.Val293=
XM_011522498.2:c.879T=	XP_011520800.1:p.Val293=
XM_017023237.1:c.879T=	XP_016878726.1:p.Val293=
XM_017023238.1:c.753T=	XP_016878727.1:p.Val251=
XM_017023239.1:c.741T=	XP_016878728.1:p.Val247=
XM_017023240.1:c.879T=	XP_016878729.1:p.Val293=
XM_017023241.1:c.615T=	XP_016878730.1:p.Val205=
XM_017023242.1:c.879T=	XP_016878731.1:p.Val293=
XM_017023243.2:c.879T=	XP_016878732.1:p.Val293=